离子色谱法测定海水中氯离子和硫酸根离子     

王丕波  曾艳敏  闫晶  殷丽娜  任登龙 《海洋科学》2020,44(11):52-56

氯离子和硫酸根离子是海水中重要的无机阴离子，在研究海洋生态变化、海洋循环作用过程与海洋全球气候变化等领域具有重要的指示意义。其测定方法较多，但缺少相应的测试方法。本文对测定海水中Cl^-，SO₄^2-的离子色谱方法进行了优化，选用IonPacAS14碳酸盐选择性离子色谱柱，以3.5 mmol/L Na₂CO₃+1 mmol/L NaHCO₃为流动相，可消除海水样品中碳酸盐及其他阴离子的干扰。该方法对Cl^-检出限为0.29 mg/L，线性相关系数r²=0.999 2，对SO₄^2-检出限为0.42 mg/L，线性相关系数r²=0.997 9。样品的加标回收率在95%~102%，Cl^-和SO₄^2-的相对标准偏差分别为1.92%和4.18%。该方法简便、迅速、灵敏、准确度高，可满足批量海水样品中Cl^-与SO₄^2-的准确测试。  相似文献   

Li₂SO₄溶液中离子间的缔合相互作用:基于密度泛函理论和分子动力学模拟的研究   总被引：1，自引：1，他引：0  

胡俊  夏斐斐  杨凤丽  郑纯智  房春晖  曾德文  易海波 《盐湖研究》2018,26(1):39-47

基于密度泛函理论,使用B3LYP/aVDZ方法对[Li_2SO_4(H_2O)_n]~0(n=0~10、18)水合团簇的结构和性质进行了系统地研究,并结合Car-Parrinello分子动力学(CPMD)模拟了不同浓度的Li_2SO_4溶液结构,目的在于理解在Li_2SO_4溶液中离子间缔合相互作用及可能存在的物种。研究发现,对于[Li_2SO_4(H_2O)_n]~0(n=0~10、18)水合团簇,双配位单齿螯合接触离子对结构比双配位双齿螯合接触离子对结构更稳定,溶剂共享离子对结构最不稳定。同时,CPMD模拟结果表明,在3.09和3.17 mol/kg的Li_2SO_4溶液中,双配位单齿螯合接触离子对结构仍然是主要物种。以上结果表明在饱和的Li_2SO_4溶液(3.16 mol/kg)中,Li~+和SO_4~(2-)离子间的相互缔合作用主要以双配位单齿螯合接触离子对结构的物种存在,而具有双配位双齿螯合离子对结构的物种占少数,溶剂共享离子对结构几乎不存在。  相似文献   

Dehydration experiments on natural omphacites: qualitative and quantitative characterization by various spectroscopic methods   总被引：1，自引：0，他引：1  

M. Koch-Müller  I. Abs-Wurmbach  D. Rhede  V. Kahlenberg  S. Matsyuk 《Physics and Chemistry of Minerals》2007,34(9):663-678

A series of natural omphacites from a wide range of P, T occurrences were investigated by electron microprobe (EMP), infrared (IR)-, Mössbauer (MS)- and optical spectroscopy in the UV/VIS spectral range (UV/VIS), secondary ion mass spectrometry (SIMS) and single crystal structure refinement by X-ray diffraction (XRD) to study the influence of hydrogen loss on valence state and site occupancies of iron. In accordance with literature data we found Fe²⁺ at M1 as well as at M2, and in a first approach assigned Fe³⁺ to M1, as indicated by MS and XRD results. Hydrogen content of three of our omphacite samples were measured by SIMS. In combination with IR spectroscopy we determined an absorption coefficient: ε _i,tot = 65,000 ± 3,000 lmol_H2O ^?1 cm^?2. Using this new ε _i,tot value, we obtained water concentrations ranging from 60 to 700 ppm H₂O (by weight). Hydrogen loss was simulated by stepwise heating the most water rich samples in air up to 800°C. After heat treatment the samples were analyzed again by IR, MS, UV/VIS, and XRD. Depending on the type of the OH defect, the grade of dehydration with increasing temperature is significantly different. In samples relatively poor in Fe³⁺ (<0.1 Fe³⁺ pfu), hydrogen associated with vacancies at M2 (OH bands around 3,450 cm^?1) starts to leave the structure at about 550°C and is completely gone at 780°C. Hydrogen associated with Al³⁺ at the tetrahedral site (OH bands around 3,525 cm^?1, Koch-Müller et al., Am Mineral, 89:921–931, 2004) remains completely unaffected by heat treatment up to 700°C. But all hydrogen vanished at about 775°C. However, this is different for a more Fe³⁺-rich sample (0.2 Fe³⁺ pfu). Its IR spectrum is characterized by a very intense OH band at 3,515 cm^?1 plus shoulder at 3,450 cm^?1. We assign this intense high-energy band to vibrations of an OH dipole associated with Fe³⁺ at M1 and a vacancy either at M1 or M2. OH release during heating is positively correlated with decrease in Fe²⁺ and combined with increase in Fe³⁺. That dehydration is correlated with oxidation of Fe²⁺ is indirectly confirmed by annealing of one sample in a gas mixing furnace at 700°C under reducing conditions keeping almost constant OH^? content and giving no indication of Fe²⁺-oxidation. Obtained data indicate that in samples with a relatively high concentration of Fe²⁺ at M2 and low-water concentrations, i.e., at a ratio of Fe^{2+ M2}/H > 10 dehydration occurs by iron oxidation of Fe²⁺ exclusively at the M2 site following the reaction: \( {\left[ {{\text{Fe}}^{{{\text{2 + [ M2]}}}}{\text{OH}}^{ - } } \right]} = {\left[ {{\text{Fe}}^{{{\text{3 + [ M2]}}}} {\text{O}}^{{{\text{2}} - }} } \right]} + {\text{1/2}}\;{\text{H}}_{{\text{2}}} \uparrow . \) In samples having relatively low concentration of Fe²⁺ at M2 but high-water concentrations, i.e., ratio of Fe^{2+ M2}/H < 5.0 dehydration occurs through oxidation of Fe²⁺ at M1.  相似文献   

南极洲伊丽莎白公主地区主要离子沉积方式及nssSO_4~(2-)气候效应研究   总被引：2，自引：1，他引：1       下载免费PDF全文

张明军  李忠勤  秦大河  效存德  康建成  李军 《极地研究》1999,11(3):161-168

通过对１９９６／１９９７年中国首次南极内陆冰盖考察获得的南极洲伊丽莎白公主地区５０ｍ 雪芯样品主要阴、阳离子浓度、通量和积累率关系的研究,揭示以下规律：１）南极洲伊丽莎白公主地区大气中各主要离子浓度足够大,足以使本地区冰雪中主要离子浓度不随积累率的变化而变化,即离子浓度不受积累率的影响。２）各主要离子干、湿沉积所占比重的计算结果表明,本地区离子沉积方式以湿沉积为主。另外,ｎｓｓＳＯ２－４ 的研究结果表明火山爆发的中、短期气候效应在伊丽莎白公主地区反应不明显。  相似文献   

柱撑粘土矿物的研究新进展——新矿物材料研究综述之一   总被引：5，自引：0，他引：5  

刘优  陆琦 《矿物岩石》1999,19(1):101-104

柱撑粘土矿物作为一种大层间距的多酸型层柱微孔材料,是一种性能优异的催化剂和吸附剂,本文在较全面分析前人资料的基础上,结合笔者所做的工作,对柱撑粘土矿物的制备性能表征及其应用最新研究进展进行综述与展望。  相似文献   

陶瓷釉矿物学特征的电子自旋共振(ESR)研究   总被引：2，自引：1，他引：1  

唐荣炳  龚国洪  尹祚莹 《矿物岩石地球化学通报》1999,(4)

早在６０年代初,Ｇｒｉｓｃｏｎ等人［１］就曾用ＥＳＲ方法对玻璃中的顺磁离子进行了研究。８０年代初Ｃａｎａｒａ等人［２］又用ＥＳＲ方法研究了硅酸玻璃、釉熔块和陶瓷色料的波谱特征,发现发色元素Ｃｒ、Ｆｅ、Ｃｏ等在釉料中的反应行为,石田等人［３］则研究了含铁高岭土和瓷胎中氧化铁的存在状态。８０年代末蔡秀成等人［４］应用ＥＳＲ方法探讨了景德镇传统“石灰碱釉”的油（煤）窑产品发黄机理。由此可见,用ＥＳＲ方法研究铁瓷釉及瓷胎中顺磁杂质离子的存在形式,对提高陶瓷质量和呈色机理的探讨有着广阔的应用前景。１　样…  相似文献   

Negative ions in the auroral mesosphere during a PCA event around sunset     

C. F. del Pozo  E. Turunen  T. Ulich 《Annales Geophysicae》1999,17(6):782-793

This is a study of the negative ion chemistry in the mesosphere above Tromsø using a number of EISCAT observations of high energy proton precipitation events during the last solar maximum, and in particular around sunset on 23 October, 1989. In these conditions it is possible to look at the relative importance of the various photodetachment and photodissociation processes controlling the concentration of negative ions. The data analysed are from several UHF GEN11 determinations of the ion-plasma ACF together with the pseudo zero-lag estimate of the ‘raw’ electron density, at heights between 55 km and 85 km, at less than 1 km resolution. The power profiles from the UHF are combined with the 55-ion Sodankylä model to obtain consistent estimates of the electron density, the negative ion concentrations, and the average ion mass with height. The neutral concentrations and ion temperature are given by the MSIS90 model. These parameters are then used to compare the calculated widths of the ion-line with the GEN11 determinations. The ion-line spectrum gives information on the effects of negative ions below 70 km where they are dominant; the spectral width is almost a direct measure of the relative abundance of negative ions.  相似文献   

离子色谱分析中的样品预处理   总被引：10，自引：0，他引：10  

田松柏 《岩矿测试》1999,18(1):77-79

总结了几种常用于离子色谱分析的样品预处理方法,其中包括流动相改性,气化分离法,离子交换法,膜技术,溶剂萃取,超临界流体萃取,固相萃取以及柱前和柱后衍生。引用主要参考文献１０篇。  相似文献   

珠江口海水密度的研究     

陈国华  纪红  谢式南  张力军  张爱滨 《中国海洋大学学报(自然科学版)》1999,(Z1)

用磁力浮沉子密度测量装置,在１５ ～２５ ℃之间的三个温度下测定了珠江口２０ 个水样的密度。结果表明,测定值皆高于相应条件下国际标准海水状态方程的计算值,在海水盐度范围０．０８～３３ ．４４６ ,密度平均偏差范围为２ ．４ ～５４．０ ×１０ － ３ｋｇ／ｍ３ 。测定密度和计算密度的偏差随盐度的降低而增大,与盐度的变化成直线相关：与（Ｃａ２ ＋ ）／Ｓ、ＳＯ４２ － ／Ｓ比和比碱度之间皆呈指数曲线相关。珠江口水样（Ｃａ２ ＋ ）／Ｃ１ 、ＳＯ４２ － ／Ｃ１ 和比碱度平均值分别超出大洋水平均值１７ ．８ ％ 、８ ．２１ ％ 和１５２ ％ ,其余的Ｎａ ＋ ／Ｃ１、Ｋ＋ ／Ｃ１ 和Ｓｒ２ ＋ ／Ｃ１ 比值与大洋水无明显差别,基本类同。珠江口海水的高碱度、高（Ｃａ２ ＋ ）／Ｃ１ 和高ＳＯ４２ － ／Ｃ１ 是造成其海水密度正偏差的主要因素。经计算机拟合,首次导出了珠江口海水密度的状态方程,该方程计算值与实验值的平均标准偏差为±２．５×１０－ ３ｋｇ／ｍ３ 。  相似文献   

STUDY FOR ABNORMAL VARIATIONS OF UNDERGROUND FLUID IN LIJIANG AREA,YUNNAN PROVINCE BEFORE LUDIAN M_S6.5 EARTHQUAKE IN 2014          下载免费PDF全文

YANG Zhu-zhuan  DENG Zhi-hui  YANG Yue-wen  DENG Sheng-chang  LI Qing 《地震地质》2018,40(2):480-498

The study is based on the underground fluid observation data in Lijiang area, northwest Yunnan Province. The data include the water level and temperature in Dangxiao well and Jinjia well, and the ion measurements in Ganze spring. Combining with the data of regional hydrogeology, rainfall, well structures, and the geothermal gradient, we analyzed the variations of each measurement item before the Ludian M_S6.5 earthquake on August 3, 2014 and discussed the possible mechanism for the abnormal variations. The water levels of both Dangxiao well and Jinjia well are influenced by local rainfall, but the former shows hysteresis according to rainy seasons and is the long trend influence; while the latter shows synchronization between high water level and rainy season, indicating good connection between well water and shallow aquifer. The recharge water for Dangxiao well is in relatively low temperature, and the temperature sensor is located at the major connecting section between the well water and the aquifer; the water temperature variation is mainly affected by the discharge status and variation of water level. The Jinjia well is always in static level, and the temperature sensor is below the major connecting section between the well water and aquifer, so the water temperature is affected little by water level variations and in smooth fluctuation. The recharge source for Ganze spring can generally increase the contents of calcium and magnesium ions, so does the conductivity. The water level data of Dangxiao well since 2012 are decomposed with wavelet technique. The results, excluding such high-frequency components as the noise and the semidiurnal and daily wave components influenced by earth tide, are further processed with difference method in order to eliminate the trend effect. The results show that the relative change of water level is enhanced and in relatively rapid increase before the Ludian M_S6.5 earthquake; the corresponding water temperature values are high. The tendency of water level in Jinjia well displays descending, while the corresponding water temperature shows ascending. The content of calcium ion, magnesium ion, bicarbonate ion, and conductivity of Ganze spring are descending, while the content of fluoride ion is ascending. The abnormal variations of underground fluid in Lijiang area appeared in turns and were accompanied with minor earthquakes before Ludian M_S6.5 earthquake, which indicates enhancing of regional stress and increasing of fluid activity.  相似文献